Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g15740 | A03 | 6725883 | G | A | upstream_gene_variant | MODIFIER | c.-4102G>A| |
S13 |
2 | BAA03g15740 | A03 | 6725907 | C | T | upstream_gene_variant | MODIFIER | c.-4078C>T| |
S280 |
3 | BAA03g15740 | A03 | 6726734 | G | A | upstream_gene_variant | MODIFIER | c.-3251G>A| |
S257 |
4 | BAA03g15740 | A03 | 6727684 | G | A | upstream_gene_variant | MODIFIER | c.-2301G>A| |
S130 |
5 | BAA03g15740 | A03 | 6727977 | C | T | upstream_gene_variant | MODIFIER | c.-2008C>T| |
S61 |
6 | BAA03g15740 | A03 | 6728090 | C | T | upstream_gene_variant | MODIFIER | c.-1895C>T| |
S35 |
7 | BAA03g15740 | A03 | 6729375 | G | A | upstream_gene_variant | MODIFIER | c.-610G>A| |
S262 S263 |
8 | BAA03g15740 | A03 | 6729611 | C | T | upstream_gene_variant | MODIFIER | c.-374C>T| |
S164 |
9 | BAA03g15740 | A03 | 6731817 | C | T | missense_variant | MODERATE | c.650C>T|p.Ser217Phe |
S66 |
10 | BAA03g15740 | A03 | 6731856 | C | T | missense_variant&splice_region_variant | MODERATE | c.689C>T|p.Ser230Leu |
S232 |
11 | BAA03g15740 | A03 | 6731884 | C | T | intron_variant | MODIFIER | c.691+26C>T| |
S110 |
12 | BAA03g15740 | A03 | 6732207 | C | T | synonymous_variant | LOW | c.882C>T|p.Val294Val |
S173 |
13 | BAA03g15740 | A03 | 6732214 | C | T | missense_variant | MODERATE | c.889C>T|p.Leu297Phe |
S129 |
14 | BAA03g15740 | A03 | 6732802 | G | A | missense_variant | MODERATE | c.1402G>A|p.Glu468Lys |
S89 |
15 | BAA03g15740 | A03 | 6733909 | G | A | synonymous_variant | LOW | c.2241G>A|p.Lys747Lys |
S267 |
16 | BAA03g15740 | A03 | 6733969 | G | A | synonymous_variant | LOW | c.2301G>A|p.Glu767Glu |
S76 |
17 | BAA03g15740 | A03 | 6738941 | C | T | downstream_gene_variant | MODIFIER | c.*4720C>T| |
S62 |